We have investigated the microstructure of a modified aluminium alloy 6082 with additions of copper and zirconium. The billets of this alloy, with the diameter of 282 mm, were semi-continuously cast using HTAS (Hot Top ? Air Slip). Samples from the bottom and head of a billet were prepared by metallographic methods, and investigated using different methods, such as light microscopy, scanning electron microscopy with microchemical analysis, differential scanning calorimetry and X-ray diffraction. The processes during solidification were modelled by using the Scheil model, which gave rather good matching with the experimental data. By analysing the results of the experiments and of the Scheil model, we proposed a probable course of solidification of the investigated alloy.
COBISS.SI-ID: 22560278
Iron core–gold shell (Fe@Au) nanoparticles are prominent for their magnetic and optical properties, which are especially beneficial for biomedical uses. Some experiments were carried out to produce Fe@Au particles with a one-step synthesis method, Ultrasonic Spray Pyrolysis (USP), which is able to produce the particles in a continuous process. The Fe@Au particles were produced with USP from a precursor solution with dissolved Iron (III) chloride and Gold (III) chloride, with Fe/Au concentration ratios ranging from 0.1 to 4. The resulting products are larger Fe oxide particles (mostly maghemite Fe2O3), with mean sizes of about 260–390 nm, decorated with Au nanoparticles (AuNPs) with mean sizes of around 24–67 nm. The Fe oxide core particles are mostly spherical in all of the experiments, while the AuNPs become increasingly irregular and more heavily agglomerated with lower Fe/Au concentration ratios in the precursor solution. The resulting particle morphology from these experiments is caused by surface chemistry and particle to solvent interactions during particle formation inside the USP system.
COBISS.SI-ID: 22656022
Colloidal gold nanoparticles (AuNPs) were prepared from two different liquid precursors (gold (III) acetate and gold (III) chloride), using the Ultrasonic Spray Pyrolysis (USP) process. The STEM characterisation showed that the AuNPs from gold chloride are spherical, with average diameters of 57.2 and 69.4 nm, while the AuNPs from gold acetate are ellipsoidal, with average diameters of 84.2 and 134.3 nm, according to Dynamic Light Scattering (DLS) measurements. UV/VIS spectroscopy revealed the maximum absorbance band of AuNPs between 532 and 560 nm, which indicates a stable state. Colloidal AuNPs were used as starting material and were mixed together with acrylic acid (AA) and acrylamide (Am) for the free radical polymerization of polyacrylate-AuNPs’ composites, with the purpose of using them for temporary cavity fillings in the dental industry. SEM characterisation of polyacrylate-AuNPs’ composites revealed a uniform distribution of AuNPs through the polymer matrix, revealing that the AuNPs remained stable during the polymerization process. The density measurements revealed that colloidal AuNPs increase the densities of the prepared polyacrylate-AuNPs’ composites; the densities were increased up to 40% in comparison with the densities of the control samples. A compressive test showed that polyacrylate-AuNPs’ composites exhibited lower compressive strength compared to the control samples, while their toughness increased. At 50% compression deformation some of the samples fracture, suggesting that incorporation of colloidal AuNPs do not improve their compressive strength, but increase their toughness significantly. This increased toughness is the measured property which makes prepared polyacrylate-AuNPs potentially useful in dentistry.
COBISS.SI-ID: 22761238
Gold nanoparticles (GNPs) have been investigated extensively as drug carriers in tumour immunotherapy in combination with photothermal therapy. For this purpose, GNPs should be stabilised in biological fluids. The goal of this study was to examine how stabilisation agents influence cytotoxicity and immune response in vitro. Spherical GNPs, 20 nm in size, were prepared by ultrasonic spray pyrolysis (USP). Three types of stabilising agents were used: sodium citrate (SC), polyvinyl-pyrrolidone (PVP), and poly-ethylene glycol (PEG). Pristine, non-stabilised GNPs were used as a control. The culture models were mouse L929 cells, B16F10 melanoma cells and human peripheral blood mononuclear cells (PBMNCs), obtained from healthy donors. Control SC- and PEG-GNPs were non-cytotoxic at concentrations (range 1–100 µg/mL), in contrast to PVP-GNPs, which were cytotoxic at higher concentrations. Control GNPs inhibited the production of IFN-? slightly, and augmented the production of IL-10 by PHA-stimulated PBMNC cultures. PEG-GNPs inhibited the production of pro-inflammatory cytokines (IL-1, IL-6, IL-8, TNF-?) and Th1-related cytokines (IFN-? and IL-12p70), and increased the production of Th2 cytokines (IL-4 and IL-5). SC-PEG inhibited the production of IL-8 and IL-17A. In contrast, PVP-GNPs stimulated the production of pro-inflammatory cytokines, Th1 cytokines, and IL-17A, but also IL-10. When uptake of GNPs by monocytes/macrophages in PBMNC cultures was analysed, the ingestion of PEG- GNPs was significantly lower compared to SC- and PVP-GNPs. In conclusion, stabilisation agents modulate biocompatibility and immune response significantly, so their adequate choice for preparation of GNPs is an important factor when considering the use of GNPs for application in vivo.
COBISS.SI-ID: 22848790
Ag@ (Y0.95 Eu0.05)2O3 nanocomposites were synthesized by single step Ultrasonic Spray Pyrolysis (USP). 800?°C synthesis temperature and 1.5?l/ min air flow were determined as optimal USP parameters. A detailed parametric study was conducted on samples with varying silver contents and heat treatment conditions. The effect of silver in both as prepared and heat treated samples were elucidated in terms of structural and functional properties. Ag incorporation decreased luminescence efficiency due to the lack of crystallization of matrix and non-homogenous distribution of Eu and Ag in as prepared samples. Heat treatment improved luminescence by improved crystal quality for all samples; however, with increasing Ag content effect of heat treatment was more pronounced owing to uniform distribution of Ag. 2.5?wt% Ag addition followed by 2?h heat treatment after USP synthesis is suggested as the most efficient nanocomposite for red light emitting down converting phosphor applications.
COBISS.SI-ID: 22316822